Variant report

Variant	rs13355434
Chromosome Location	chr5:49871733-49871734
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 68 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs10038842	1.00[ASN][1000 genomes]
rs10039639	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs10041633	1.00[ASN][1000 genomes]
rs10043477	1.00[ASN][1000 genomes]
rs10045122	1.00[ASN][1000 genomes]
rs10052001	1.00[ASN][1000 genomes]
rs10070517	1.00[ASN][1000 genomes]
rs10071272	1.00[ASN][1000 genomes]
rs10434558	0.91[ASW][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.92[MEX][hapmap];0.90[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10461587	0.83[EUR][1000 genomes]
rs10471888	1.00[ASN][1000 genomes]
rs10471893	1.00[ASN][1000 genomes]
rs10471940	1.00[ASN][1000 genomes]
rs10471956	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11741205	1.00[ASN][1000 genomes]
rs12518710	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13162921	1.00[ASN][1000 genomes]
rs13164951	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs13355372	1.00[ASN][1000 genomes]
rs1375127	1.00[ASN][1000 genomes]
rs1988613	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs2034392	1.00[ASN][1000 genomes]
rs2034394	1.00[ASN][1000 genomes]
rs26068	1.00[ASN][1000 genomes]
rs2697662	1.00[ASN][1000 genomes]
rs282549	1.00[ASN][1000 genomes]
rs282552	1.00[JPT][hapmap]
rs282559	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs35667121	0.88[EUR][1000 genomes]
rs4029420	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4101529	1.00[ASN][1000 genomes]
rs4572006	0.89[EUR][1000 genomes]
rs4865846	1.00[ASN][1000 genomes]
rs4865974	1.00[JPT][hapmap]
rs4866001	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6450359	1.00[ASN][1000 genomes]
rs6863162	0.89[EUR][1000 genomes]
rs6868550	0.88[EUR][1000 genomes]
rs6869356	1.00[ASN][1000 genomes]
rs6879306	1.00[ASN][1000 genomes]
rs6883718	0.88[EUR][1000 genomes]
rs6886872	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6887758	0.88[EUR][1000 genomes]
rs6888147	1.00[ASN][1000 genomes]
rs6893665	0.90[EUR][1000 genomes]
rs73093361	1.00[ASN][1000 genomes]
rs73112331	1.00[ASN][1000 genomes]
rs73112340	1.00[ASN][1000 genomes]
rs7449019	1.00[ASN][1000 genomes]
rs7709831	1.00[ASN][1000 genomes]
rs7710150	1.00[ASN][1000 genomes]
rs7711839	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7723361	1.00[JPT][hapmap]
rs7728222	1.00[ASN][1000 genomes]
rs7730847	1.00[ASN][1000 genomes]
rs7734389	1.00[ASN][1000 genomes]
rs895801	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs921210	1.00[JPT][hapmap];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032003	chr5:49455624-49881491	Strong transcription Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1016583	chr5:49455624-50116720	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1023140	chr5:49455624-50121623	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1022067	chr5:49584188-49960083	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv537758	chr5:49584188-49960083	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv918220	chr5:49584188-50111282	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv931010	chr5:49584189-50118254	Genic enhancers Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv523212	chr5:49597497-50058043	Enhancers Genic enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	esv2757995	chr5:49748352-50058182	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
10	esv2759342	chr5:49748352-50058182	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs13355434	PARP8	Cis_1M	lymphoblastoid	RTeQTL
rs13355434	LOC647121	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:49870000-49872400	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr5:49870000-49873000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
3	chr5:49870000-49873200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr5:49870000-49873200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr5:49870400-49872200	Enhancers	Dnd41	blood
6	chr5:49870800-49871800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr5:49870800-49872200	Weak transcription	Monocytes-CD14+_RO01746	blood
8	chr5:49871200-49872000	Enhancers	Primary T killer memory cells from peripheral blood	blood
9	chr5:49871400-49872600	Weak transcription	Primary T cells fromperipheralblood	blood
10	chr5:49871400-49873200	Enhancers	Primary T helper naive cells from peripheral blood	blood
11	chr5:49871600-49871800	Enhancers	Primary T helper cells PMA-I stimulated	--

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